Canonical Allele Identifier: CA391931829
Gene: SPRED1 HGNC NCBI

Linked Data

dbSNP Id: rs1490356893

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253202C>A , CM000677.2:g.38253202C>A GRCh38
NC_000015.9:g.38545403C>A , CM000677.1:g.38545403C>A GRCh37
NC_000015.8:g.36332695C>A NCBI36
NG_008980.1:g.5352C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.17C>A MANE Select ENSP00000299084.4:p.Ala6Glu
ENST00000299084.8:c.17C>A ENSP00000299084.4:p.Ala6Glu
ENST00000561205.1:n.355C>A
ENST00000561317.1:c.-111C>A ENSP00000453680.1:n.-111C>A
NM_152594.2:c.17C>A NP_689807.1:p.Ala6Glu
XM_005254202.2:c.17C>A XP_005254259.1:p.Ala6Glu
XM_005254203.3:c.-31C>A XP_005254260.1:n.-31C>A
XM_005254202.3:c.17C>A XP_005254259.1:p.Ala6Glu
XR_001751484.1:n.87+365G>T
NM_152594.3:c.17C>A MANE Select NP_689807.1:p.Ala6Glu